A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936657



Internal ID25154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86908927..86939977hg38UCSC Ensembl
chr3:86958077..86989127hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3831051
hg1931051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436727
Supporting Variants
Samples
Known GenesVGLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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